Detail Information of Genetic Polymorphisms
General Information of Drug Transporter (DT) | |||||
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DT ID | DTD0648 Transporter Info | ||||
Gene Name | ATP7A | ||||
Protein Name | Copper-transporting ATPase 1 | ||||
Gene ID | |||||
UniProt ID | |||||
Genetic Polymorphisms of DT (GPD) | |||||
Genetic Polymorphism | rs2227291 | ||||
Site of GPD | chrX:78013005 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>C | ||||
Minor Allele Frequency | G=0.7080/1401 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Docetaxel | N.A. | Sedation | Allele G is associated with increased risk of toxicity when treated with docetaxel and thalidomide in people with Prostatic Neoplasms as compared to allele C. | [ 1] | |
Thalidomide | N.A. | Sedation | Allele G is associated with increased risk of toxicity when treated with docetaxel and thalidomide in people with Prostatic Neoplasms as compared to allele C. | [ 1] | |
Docetaxel | N.A. | Prostatic Neoplasms | Allele G is associated with increased risk of toxicity when treated with docetaxel and thalidomide in people with Prostatic Neoplasms as compared to allele C. | [ 1] | |
Thalidomide | N.A. | Prostatic Neoplasms | Allele G is associated with increased risk of toxicity when treated with docetaxel and thalidomide in people with Prostatic Neoplasms as compared to allele C. | [ 1] | |
Genotype CC | Click to Show/Hide the Full List of Affected Drugs: 2 Drugs in Total | ||||
Docetaxel | N.A. | Prostatic Neoplasms | Patients with the CC genotype may have decreased but not absent risk of toxicity with docetaxel and thalidomide as compared to patients with the CG or GG genotypes. Other genetic and clinical factors may also influence treatment response. | [ 1] | |
Thalidomide | N.A. | Prostatic Neoplasms | Patients with the CC genotype may have decreased but not absent risk of toxicity with docetaxel and thalidomide as compared to patients with the CG or GG genotypes. Other genetic and clinical factors may also influence treatment response. | [ 1] | |
Genotype CG | Click to Show/Hide the Full List of Affected Drugs: 2 Drugs in Total | ||||
Docetaxel | N.A. | Prostatic Neoplasms | Patients with the CG genotype may have an increased risk of toxicity with docetaxel and thalidomide as compared to patients with the CC genotype. Other genetic and clinical factors may also influence treatment response. | [ 1] | |
Thalidomide | N.A. | Prostatic Neoplasms | Patients with the CG genotype may have an increased risk of toxicity with docetaxel and thalidomide as compared to patients with the CC genotype. Other genetic and clinical factors may also influence treatment response. | [ 1] | |
Genotype GG | Click to Show/Hide the Full List of Affected Drugs: 2 Drugs in Total | ||||
Docetaxel | N.A. | Prostatic Neoplasms | Patients with the GG genotype may have an increased risk of toxicity with docetaxel and thalidomide as compared to patients with the CC genotype. Other genetic and clinical factors may also influence treatment response. | [ 1] | |
Thalidomide | N.A. | Prostatic Neoplasms | Patients with the GG genotype may have an increased risk of toxicity with docetaxel and thalidomide as compared to patients with the CC genotype. Other genetic and clinical factors may also influence treatment response. | [ 1] | |
References | |||||
1 | A pharmacogenetic study of docetaxel and thalidomide in patients with castration-resistant prostate cancer using the DMET genotyping platform. Pharmacogenomics J. 2010 Jun;10(3):191-9. |
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